List of variants in gene combination SCN1A, SCN9A reported as not provided for Primary erythromelalgia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.3481= (p.Trp1161=)	rs6746030	0.12070
NM_001365536.1(SCN9A):c.1185C>A (p.Asn395Lys)	rs80356471
NM_001365536.1(SCN9A):c.1198G>A (p.Val400Met)	rs1553491169
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr)	rs41268673
NM_001365536.1(SCN9A):c.2501T>G (p.Leu834Arg)	rs80356473
NM_001365536.1(SCN9A):c.2576T>C (p.Ile859Thr)	rs80356474
NM_001365536.1(SCN9A):c.2605C>T (p.Leu869Phe)	rs80356476
NM_001365536.1(SCN9A):c.2606T>A (p.Leu869His)	rs80356475
NM_001365536.1(SCN9A):c.2620G>C (p.Ala874Pro)	rs80356477
NM_001365536.1(SCN9A):c.4378T>G (p.Phe1460Val)	rs80356478

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.